A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033534



Internal ID18776067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:34548811..34588192hg38UCSC Ensembl
Innerchr6:34516588..34555969hg19UCSC Ensembl
Innerchr6:34624566..34663947hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3839382
hg1939382
hg1839382
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3657369
Samples
Known GenesC6orf106, SPDEF
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033534
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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